Persistence of Protection Against Hepatitis B Virus Infection Among Adolescents Vaccinated With Recombinant Hepatitis B Vaccine Beginning at Birth: A 15-Year Follow-Up Study
BACKGROUND:Long-term follow-up studies of populations that received recombinant hepatitis B (HB) vaccination beginning at birth are limited. METHODS:Micronesian adolescents who had received 3 doses of recombinant HB vaccine (Recombivax 5 μg at birth, 2.5 μg at 2 months, 2.5 μg at 6 months) and teste...
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Veröffentlicht in: | The Pediatric infectious disease journal 2008-10, Vol.27 (10), p.881-885 |
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creator | Bialek, Stephanie R Bower, William A Novak, Ryan Helgenberger, Louisa Auerbach, Steven B Williams, Ian T Bell, Beth P |
description | BACKGROUND:Long-term follow-up studies of populations that received recombinant hepatitis B (HB) vaccination beginning at birth are limited.
METHODS:Micronesian adolescents who had received 3 doses of recombinant HB vaccine (Recombivax 5 μg at birth, 2.5 μg at 2 months, 2.5 μg at 6 months) and tested negative for antibody to HB core antigen (anti-HBc) 2 years after primary vaccination (baseline testing) were followed up 15 years after primary vaccination. After testing for anti-HBc, HB surface antigen (HBsAg), and antibody to HBsAg (anti-HBs), participants received a booster dose of HB vaccine. An anamnestic response was defined as an increase in anti-HBs concentrations to a level ≥10 mIU/mL 14 days postbooster.
RESULTS:Of the 105 participants, 42 (40.0%) had anti-HBs concentrations ≥10 mIU/mL on baseline testing. At 15 years, 8 (7.6%) were anti-HBc positive; none were HBsAg positive. Of the remaining 97, 7 (7.3%) had anti-HBs concentrations ≥10 mIU/mL. Of the 96 who received a booster dose, 46 (47.9%) had an anamnestic response; final antibody concentrations were 10-99 mIU/mL for 17 (17.7%) and >100 mIU/mL for 29 (30.2%). Participants with anti-HBs concentrations ≥10 mIU/mL on baseline testing were more likely to have an anamnestic response at 15 years [26/39 (66.7%) versus 20/57 (35.1%); P = 0.003].
CONCLUSIONS:Fifteen years after primary vaccination starting at birth, 8% of participants had evidence of past HB virus infection, but none had chronic infection. Absence of an anamnestic response to an additional vaccine dose, seen in half of participants, might indicate waning immunity. |
doi_str_mv | 10.1097/INF.0b013e31817702ba |
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METHODS:Micronesian adolescents who had received 3 doses of recombinant HB vaccine (Recombivax 5 μg at birth, 2.5 μg at 2 months, 2.5 μg at 6 months) and tested negative for antibody to HB core antigen (anti-HBc) 2 years after primary vaccination (baseline testing) were followed up 15 years after primary vaccination. After testing for anti-HBc, HB surface antigen (HBsAg), and antibody to HBsAg (anti-HBs), participants received a booster dose of HB vaccine. An anamnestic response was defined as an increase in anti-HBs concentrations to a level ≥10 mIU/mL 14 days postbooster.
RESULTS:Of the 105 participants, 42 (40.0%) had anti-HBs concentrations ≥10 mIU/mL on baseline testing. At 15 years, 8 (7.6%) were anti-HBc positive; none were HBsAg positive. Of the remaining 97, 7 (7.3%) had anti-HBs concentrations ≥10 mIU/mL. Of the 96 who received a booster dose, 46 (47.9%) had an anamnestic response; final antibody concentrations were 10-99 mIU/mL for 17 (17.7%) and >100 mIU/mL for 29 (30.2%). Participants with anti-HBs concentrations ≥10 mIU/mL on baseline testing were more likely to have an anamnestic response at 15 years [26/39 (66.7%) versus 20/57 (35.1%); P = 0.003].
CONCLUSIONS:Fifteen years after primary vaccination starting at birth, 8% of participants had evidence of past HB virus infection, but none had chronic infection. Absence of an anamnestic response to an additional vaccine dose, seen in half of participants, might indicate waning immunity.</description><identifier>ISSN: 0891-3668</identifier><identifier>EISSN: 1532-0987</identifier><identifier>DOI: 10.1097/INF.0b013e31817702ba</identifier><identifier>PMID: 18756185</identifier><identifier>CODEN: PIDJEV</identifier><language>eng</language><publisher>Baltimore, MD: Lippincott Williams & Wilkins, Inc</publisher><subject>Adolescent ; Biological and medical sciences ; Female ; Follow-Up Studies ; Hepatitis B - immunology ; Hepatitis B - prevention & control ; Hepatitis B Antibodies - blood ; Hepatitis B Antibodies - immunology ; Hepatitis B Core Antigens - blood ; Hepatitis B Core Antigens - immunology ; Hepatitis B Surface Antigens - blood ; Hepatitis B Surface Antigens - immunology ; Hepatitis B Vaccines - administration & dosage ; Hepatitis B Vaccines - immunology ; Human viral diseases ; Humans ; Immunization Schedule ; Immunization, Secondary ; Immunologic Memory ; Infant ; Infectious diseases ; Male ; Medical sciences ; Vaccines, Synthetic - administration & dosage ; Vaccines, Synthetic - immunology ; Viral diseases ; Viral hepatitis</subject><ispartof>The Pediatric infectious disease journal, 2008-10, Vol.27 (10), p.881-885</ispartof><rights>2008 Lippincott Williams & Wilkins, Inc.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2445-14f5a47560dfcb3c7acc14e22277e39a9f77c0260417814a9b31cb1dafa555753</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20691641$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18756185$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bialek, Stephanie R</creatorcontrib><creatorcontrib>Bower, William A</creatorcontrib><creatorcontrib>Novak, Ryan</creatorcontrib><creatorcontrib>Helgenberger, Louisa</creatorcontrib><creatorcontrib>Auerbach, Steven B</creatorcontrib><creatorcontrib>Williams, Ian T</creatorcontrib><creatorcontrib>Bell, Beth P</creatorcontrib><title>Persistence of Protection Against Hepatitis B Virus Infection Among Adolescents Vaccinated With Recombinant Hepatitis B Vaccine Beginning at Birth: A 15-Year Follow-Up Study</title><title>The Pediatric infectious disease journal</title><addtitle>Pediatr Infect Dis J</addtitle><description>BACKGROUND:Long-term follow-up studies of populations that received recombinant hepatitis B (HB) vaccination beginning at birth are limited.
METHODS:Micronesian adolescents who had received 3 doses of recombinant HB vaccine (Recombivax 5 μg at birth, 2.5 μg at 2 months, 2.5 μg at 6 months) and tested negative for antibody to HB core antigen (anti-HBc) 2 years after primary vaccination (baseline testing) were followed up 15 years after primary vaccination. After testing for anti-HBc, HB surface antigen (HBsAg), and antibody to HBsAg (anti-HBs), participants received a booster dose of HB vaccine. An anamnestic response was defined as an increase in anti-HBs concentrations to a level ≥10 mIU/mL 14 days postbooster.
RESULTS:Of the 105 participants, 42 (40.0%) had anti-HBs concentrations ≥10 mIU/mL on baseline testing. At 15 years, 8 (7.6%) were anti-HBc positive; none were HBsAg positive. Of the remaining 97, 7 (7.3%) had anti-HBs concentrations ≥10 mIU/mL. Of the 96 who received a booster dose, 46 (47.9%) had an anamnestic response; final antibody concentrations were 10-99 mIU/mL for 17 (17.7%) and >100 mIU/mL for 29 (30.2%). Participants with anti-HBs concentrations ≥10 mIU/mL on baseline testing were more likely to have an anamnestic response at 15 years [26/39 (66.7%) versus 20/57 (35.1%); P = 0.003].
CONCLUSIONS:Fifteen years after primary vaccination starting at birth, 8% of participants had evidence of past HB virus infection, but none had chronic infection. Absence of an anamnestic response to an additional vaccine dose, seen in half of participants, might indicate waning immunity.</description><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Hepatitis B - immunology</subject><subject>Hepatitis B - prevention & control</subject><subject>Hepatitis B Antibodies - blood</subject><subject>Hepatitis B Antibodies - immunology</subject><subject>Hepatitis B Core Antigens - blood</subject><subject>Hepatitis B Core Antigens - immunology</subject><subject>Hepatitis B Surface Antigens - blood</subject><subject>Hepatitis B Surface Antigens - immunology</subject><subject>Hepatitis B Vaccines - administration & dosage</subject><subject>Hepatitis B Vaccines - immunology</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immunization Schedule</subject><subject>Immunization, Secondary</subject><subject>Immunologic Memory</subject><subject>Infant</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Vaccines, Synthetic - administration & dosage</subject><subject>Vaccines, Synthetic - immunology</subject><subject>Viral diseases</subject><subject>Viral hepatitis</subject><issn>0891-3668</issn><issn>1532-0987</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkcFuEzEQhi0EoqHwBgj5ArctnrW93uWWVIRGqqACWsRp5fXOJoaNHWyvoj4U74hDA5V6GWusb_7R6CPkJbAzYI16u_q4PGMdA44calCKlZ1-RGYgeVmwplaPyYzVDRS8quoT8izGH4wxLoA9JSdQK1lBLWfk9xWGaGNCZ5D6gV4Fn9Ak6x2dr7V1MdEL3Olkk410QW9smCJdueEfs_VuTee9HzEadCnSG22MdTphT7_ZtKGf0fhtl3_cg6S_HNIFrq1zNqfoRBc2pM07Oqcgi--oA136cfT74npHv6Spv31Ongx6jPji-J6S6-X7r-cXxeWnD6vz-WVhSiFkAWKQWuQTWT-YjhuVd4HAsiyVQt7oZlDKsLJiAlQNQjcdB9NBrwctpVSSn5I3d7m74H9NGFO7tfm-cdQO_RTbqqmAV9BkUNyBJvgYAw7tLtitDrctsPagqc2a2oea8tirY_7UbbG_Hzp6ycDrI6Cj0eMQtDM2_udKVjVQCbjfv_djyiZ_jtMeQ7tBPaZNm4WzSkhRlIzVcOiKQ5H8Dw8xrKQ</recordid><startdate>200810</startdate><enddate>200810</enddate><creator>Bialek, Stephanie R</creator><creator>Bower, William A</creator><creator>Novak, Ryan</creator><creator>Helgenberger, Louisa</creator><creator>Auerbach, Steven B</creator><creator>Williams, Ian T</creator><creator>Bell, Beth P</creator><general>Lippincott Williams & Wilkins, Inc</general><general>Lippincott</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200810</creationdate><title>Persistence of Protection Against Hepatitis B Virus Infection Among Adolescents Vaccinated With Recombinant Hepatitis B Vaccine Beginning at Birth: A 15-Year Follow-Up Study</title><author>Bialek, Stephanie R ; Bower, William A ; Novak, Ryan ; Helgenberger, Louisa ; Auerbach, Steven B ; Williams, Ian T ; Bell, Beth P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2445-14f5a47560dfcb3c7acc14e22277e39a9f77c0260417814a9b31cb1dafa555753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adolescent</topic><topic>Biological and medical sciences</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Hepatitis B - immunology</topic><topic>Hepatitis B - prevention & control</topic><topic>Hepatitis B Antibodies - blood</topic><topic>Hepatitis B Antibodies - immunology</topic><topic>Hepatitis B Core Antigens - blood</topic><topic>Hepatitis B Core Antigens - immunology</topic><topic>Hepatitis B Surface Antigens - blood</topic><topic>Hepatitis B Surface Antigens - immunology</topic><topic>Hepatitis B Vaccines - administration & dosage</topic><topic>Hepatitis B Vaccines - immunology</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Immunization Schedule</topic><topic>Immunization, Secondary</topic><topic>Immunologic Memory</topic><topic>Infant</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Vaccines, Synthetic - administration & dosage</topic><topic>Vaccines, Synthetic - immunology</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bialek, Stephanie R</creatorcontrib><creatorcontrib>Bower, William A</creatorcontrib><creatorcontrib>Novak, Ryan</creatorcontrib><creatorcontrib>Helgenberger, Louisa</creatorcontrib><creatorcontrib>Auerbach, Steven B</creatorcontrib><creatorcontrib>Williams, Ian T</creatorcontrib><creatorcontrib>Bell, Beth P</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Pediatric infectious disease journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bialek, Stephanie R</au><au>Bower, William A</au><au>Novak, Ryan</au><au>Helgenberger, Louisa</au><au>Auerbach, Steven B</au><au>Williams, Ian T</au><au>Bell, Beth P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Persistence of Protection Against Hepatitis B Virus Infection Among Adolescents Vaccinated With Recombinant Hepatitis B Vaccine Beginning at Birth: A 15-Year Follow-Up Study</atitle><jtitle>The Pediatric infectious disease journal</jtitle><addtitle>Pediatr Infect Dis J</addtitle><date>2008-10</date><risdate>2008</risdate><volume>27</volume><issue>10</issue><spage>881</spage><epage>885</epage><pages>881-885</pages><issn>0891-3668</issn><eissn>1532-0987</eissn><coden>PIDJEV</coden><abstract>BACKGROUND:Long-term follow-up studies of populations that received recombinant hepatitis B (HB) vaccination beginning at birth are limited.
METHODS:Micronesian adolescents who had received 3 doses of recombinant HB vaccine (Recombivax 5 μg at birth, 2.5 μg at 2 months, 2.5 μg at 6 months) and tested negative for antibody to HB core antigen (anti-HBc) 2 years after primary vaccination (baseline testing) were followed up 15 years after primary vaccination. After testing for anti-HBc, HB surface antigen (HBsAg), and antibody to HBsAg (anti-HBs), participants received a booster dose of HB vaccine. An anamnestic response was defined as an increase in anti-HBs concentrations to a level ≥10 mIU/mL 14 days postbooster.
RESULTS:Of the 105 participants, 42 (40.0%) had anti-HBs concentrations ≥10 mIU/mL on baseline testing. At 15 years, 8 (7.6%) were anti-HBc positive; none were HBsAg positive. Of the remaining 97, 7 (7.3%) had anti-HBs concentrations ≥10 mIU/mL. Of the 96 who received a booster dose, 46 (47.9%) had an anamnestic response; final antibody concentrations were 10-99 mIU/mL for 17 (17.7%) and >100 mIU/mL for 29 (30.2%). Participants with anti-HBs concentrations ≥10 mIU/mL on baseline testing were more likely to have an anamnestic response at 15 years [26/39 (66.7%) versus 20/57 (35.1%); P = 0.003].
CONCLUSIONS:Fifteen years after primary vaccination starting at birth, 8% of participants had evidence of past HB virus infection, but none had chronic infection. Absence of an anamnestic response to an additional vaccine dose, seen in half of participants, might indicate waning immunity.</abstract><cop>Baltimore, MD</cop><cop>Philadelphia, PA</cop><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>18756185</pmid><doi>10.1097/INF.0b013e31817702ba</doi><tpages>5</tpages></addata></record> |
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subjects | Adolescent Biological and medical sciences Female Follow-Up Studies Hepatitis B - immunology Hepatitis B - prevention & control Hepatitis B Antibodies - blood Hepatitis B Antibodies - immunology Hepatitis B Core Antigens - blood Hepatitis B Core Antigens - immunology Hepatitis B Surface Antigens - blood Hepatitis B Surface Antigens - immunology Hepatitis B Vaccines - administration & dosage Hepatitis B Vaccines - immunology Human viral diseases Humans Immunization Schedule Immunization, Secondary Immunologic Memory Infant Infectious diseases Male Medical sciences Vaccines, Synthetic - administration & dosage Vaccines, Synthetic - immunology Viral diseases Viral hepatitis |
title | Persistence of Protection Against Hepatitis B Virus Infection Among Adolescents Vaccinated With Recombinant Hepatitis B Vaccine Beginning at Birth: A 15-Year Follow-Up Study |
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